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CAS 1004775-34-1

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B-[4-(Difluoromethoxy)-2-fluorophenyl]boronic acid

Description:
B-[4-(Difluoromethoxy)-2-fluorophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with both difluoromethoxy and fluorine groups, contributing to its unique electronic properties and potential reactivity. The difluoromethoxy group enhances the compound's lipophilicity and may influence its interactions in biological systems. Boronic acids are often utilized in organic synthesis, particularly in cross-coupling reactions, and can serve as important intermediates in the development of pharmaceuticals. The presence of multiple fluorine atoms typically increases the compound's stability and alters its solubility characteristics. Additionally, the compound's structure suggests potential applications in medicinal chemistry, particularly in the design of inhibitors or modulators of biological targets. Overall, B-[4-(Difluoromethoxy)-2-fluorophenyl]boronic acid exemplifies the versatility of boronic acids in synthetic chemistry and their relevance in drug discovery.
Formula:C7H6BF3O3
InChI:InChI=1S/C7H6BF3O3/c9-6-3-4(14-7(10)11)1-2-5(6)8(12)13/h1-3,7,12-13H
InChI key:InChIKey=PLPKXPNIMSNXAF-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=C(OC(F)F)C=C1
Synonyms:
  • B-[4-(Difluoromethoxy)-2-fluorophenyl]boronic acid
  • 4-Difluoromethoxy-2-fluorobenzeneboronic acid
  • 4-Difluoromethoxy-2-fluorophenylboronic acid
  • Boronic acid, B-[4-(difluoromethoxy)-2-fluorophenyl]-
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